ライフサイエンスコーパス: snout

1 resented simultaneously on both sides of the snout.

2 delivered to a cold-sensitive region of the snout.

3 ned array of whiskers and sinus hairs on the snout.

4 tribution of whiskers and sinus hairs on the snout.

5 sed along the representation of the glabrous snout.

6 ystacial vibrissae, lower jaw, and glaborous snout.

7 ic projections from whiskers on the rodent's snout.

8 nd transverse compression of the spinosaurid snout.

9 d by cleft palate and short limbs, tail, and snout.

10 ls that corresponded to the vibrissae on the snout.

11 fields were often small, especially for the snout.

12 showed fully penetrant cleft lips and short snouts.

13 s compared to taxa with broader, more robust snouts.

14 resulted in relatively longer hindlimbs and snouts.

15 this Bauplan, possessing an extremely blunt snout, a tall, rounded skull, an anteriorly shifted jaw

16 d to representing the perioral hairs and the snout and also that neurons within this representation h

17 restrial diapsid reptiles, including a short snout and body trunk.

18 aging, bioluminescence being detected in the snout and lungs of infected mice after nasal inoculation

19 ed during the Jurassic, before the elongated snout and other fish-eating adaptations in the skull.

20 ere tuned to the distance between the animal snout and the contralateral wall, with monotonic, unimod

21 ical relevance of orienting movements of the snout and the whiskers in these animals.

22 trusion, the proximodistal shortening of the snout and widening of the hard palate is common to brach

23 FKO mice exhibit shortened snouts and wide-set eyes that become apparent at postnat

24 feeding strikes occur (above the end of the snout), and permits syngnathid fish to approach highly s

25 strictly synchronous and symmetric about the snout, and it is thought to be controlled by a brainstem

26 found in some non-ocular tissues, i.e. ears, snout, and limbs of embryos of E13.5 and E14.5 but was n

27 taining dermal lesions appeared on the ears, snout, and perianal regions of transgenic mice by the ag

28 The most prominent defects in FKO snouts are (1) a lack of growth within the frontonasal s

29 electrical stimulation of the contralateral snout as well as changes in DC-coupled potential were mo

30 m Mongolia seem to indicate a divergent long-snouted body plan among some derived tyrannosaurids, but

31 s and fatty acid synthesis in juvenile blunt snout bream.

32 bility, and paedomorphic skulls with reduced snouts but enlarged eyes and brains.

33 tes that Alioramus is a small, gracile, long-snouted carnivore that deviates from other tyrannosaurid

34 own feeding ecology for both African slender-snouted crocodile and alligator, and suggest that the sp

35 s: two longistrine taxa, the African slender-snouted crocodile Mecistops cataphractus and the Indian

36 Results show that African slender-snouted crocodile skulls are more resistant to bending t

37 determined from the ratio of tusk length to snout dimensions.

38 er fragment showed expression in the cornea, snout, dorsal fin, and tail fin of 3-day-old zebrafish l

39 m of craniofacial defects, including shorter snout, expansion of the facial midline, cleft lip, exten

40 and crusts occurred predominantly around the snout, eyes, and on ears.

41 ies and Food, Atrophic Rhinitis: a System of Snout Grading, 1978).

42 contingent upon the presence of the animal's snout in a nosepoke apparatus at the target time, as an

43 tion of running or upon the insertion of the snout into the food cup.

44 length (P < 0.05) and face width relative to snout length (P < 0.01) were present in the 44-cM region

45 sults confirmed QTLs, determining that short snout length (P < 0.05) and face width relative to snout

46 variance in relative limb length and 33% of snout length across species.

47 ignificant logarithm-of-odds (LOD) score for snout length on mouse chromosome 12 at 44 centimorgan (c

48 ation between the larval period and limb and snout lengths, mirroring the effects of within-species p

49 rences in phylogenetically conserved traits (snout morphology and body size) were consistently linked

50 Alioramus individuals, showing that the long-snouted morphology was not a transient juvenile conditio

51 or the synchronization of vibrissa, pad, and snout movements, as well as for the bilateral synchroniz

52 s devoted to representation of the glaborous snout, mystacial vibrissae, lower jaw, and oral cavity (

53 J (short snout/wide face) and C57BL/6J (long snout/narrow face), revealed a significant logarithm-of-

54 rs: they follow along walls, and "dab" their snouts on the ground at frequencies related to the whisk

55 ealing of tongue ulcers in mice subjected to snout-only irradiation.

56 When whiskers on the snout or the sensory nerves innervating them are damaged

57 sox9 essential functions, including the jaw/snout region, otic vesicle, eye, and brain.

58 -side deviation of their facial skeleton and snout regions; 4 x 2 ANOVA and post hoc t-tests revealed

59 In contrast to these results, grafts of snout skin yielded many melanomas, each originating from

60 d at the representation of the vibrissae and snout, so that the orientation of S2 formed an upright r

61 s not a transient juvenile condition of deep-snouted species, but a characteristic of a major tyranno

62 On the snout, sustained robust replication of 17tBTK(-) in the

63 ly in response to tactile stimulation of the snout, this property was not related to activity associa

64 tetrapods, most under 1 meter in length from snout to tail, radiated to dominate postextinction ecosy

65 growth rate and the strength of selection on snout to vent length.

66 we describe a remarkable new species of long-snouted tyrannosaurid from the Maastrichtian of southeas

67 olateral defects including narrow, elongated snouts, underdeveloped lower jaw and a high incidence of

68 ntonasal sutures, and (2) a reduction in the snout vasculature.

69 rs and American toads and was dependent upon snout-vent length in western toads, American toads, and

70 arkedly reduced virus titers in the skin and snout, whereas parenteral treatment did not, suggesting

71 deed, Asph-knockout mice had a foreshortened snout, which corresponds to the facial abnormalities in

72 cited by electrical stimulation of the swine snout, which is somatotopically represented in the rostr

73 F2 progeny of 2 mouse strains, DBA/2J (short snout/wide face) and C57BL/6J (long snout/narrow face),

74 These include an elongate snout with an array of conical teeth, a dorsoventrally f

75 f Cartorhynchus with which it shares a short snout with rostrally extended nasals.

76 they protract their whiskers in front of the snout without large movements.